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Updated: Apr 28, 2026

Synthesis of pH Dependent Pyrazole, Imidazole, and Isoindolone Dipyrrinone Fluorophores using a Claisen-Schmidt Condensation Approach
Published on: June 10, 2021
Arylpyrrole oligomers as tunable anion receptors
Wim Van Rossom1, Tatyana G Terentyeva, Keitaro Sodeyama
1World Premier International (WPI), Research Center for Materials Nanoarchitectonics (MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, 305-0044 Ibaraki, Japan. wimvanrossom@gmail.com jonathan.hill@nims.go.jp.
Abstract:
A novel type of arylpyrrole oligomer possessing an appropriate electropositive cavity has been designed, prepared and analysed for use as readily accessible receptors for negatively charged guests. Affinities of the receptors for various anions were determined by UV/Vis titration experiments and in depth insights into the host-guest interactions were gained by performing (1)H NMR titration experiments and X-ray crystallographic structure analyses. Experimentally determined association constants were correlated with the calculated maximum electrostatic potentials of the electropositive cavities of the receptors, allowing estimation of the strengths of host-guest associations in similar compounds. The joint contribution of aryl C-H and pyrrole N-H hydrogens was shown to be key to a strong guest association, resulting in the arylpyrrole oligomers being efficient anion receptors.
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